K903626 is an FDA 510(k) clearance for the BIOMEK AUTOMATED LABORATORY WORKSTATION W/GENELISA. This device is classified as a Analyzer, Chemistry, Centrifugal, For Clinical Use (Class I - General Controls, product code JJG).
Submitted by Beckman Instruments, Inc. (Fullerton, US). The FDA issued a Cleared decision on October 15, 1990, 66 days after receiving the submission on August 10, 1990.
This device falls under the Chemistry FDA review panel. Regulated under 21 CFR 862.2140.
| 510(k) Number | K903626 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | August 10, 1990 |
| Decision Date | October 15, 1990 |
| Days to Decision | 66 days |
| Submission Type | Traditional |
| Review Panel | Chemistry (CH) |
| Summary | — |
| Product Code | JJG — Analyzer, Chemistry, Centrifugal, For Clinical Use |
| Device Class | Class I - General Controls |
| CFR Regulation | 21 CFR 862.2140 |